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Search Thermo Fisher Scientific
CACCTGGCACAGCAGGCCTGGGGCT[C/T]GGGTCCCAGCCCAGCAGCTGTGGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612346 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GGT1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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GGT1 - gamma-glutamyltransferase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288833.1 | 951 | Intron | NP_001275762.1 | |||
NM_013421.2 | 951 | Intron | NP_038265.2 | |||
NM_013430.2 | 951 | Intron | NP_038347.2 |
LRRC75B - leucine rich repeat containing 75B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_207644.2 | 951 | Missense Mutation | NP_997527.2 | |||
XM_005261600.2 | 951 | Intron | XP_005261657.1 |